Abstract: A system for holding a slide. The system includes a housing having a side wall and a top. The top includes a recess surrounded by an outer rim. The system also includes an inlet port in communication with the recess and an elevating mechanism capable of receiving the slide and for raising the slide toward the top of the housing to engage the slide with the outer rim to form an analytical cavity. Together these elements form an analytical cavity in which the assay may be performed.

Abstract: Slideholders which are useful for manually or automatically processing biological samples on microscope slides are described. These slideholders hold multiple slides and are designed in conjunction with specialized trays for rapidly processing the mounted biological samples such as for immunocytochemical staining. The slideholder plus tray assemblies incorporate several useful advantages including a requirement for minimal reaction fluid volumes, ease of handling several slides concurrently, prevention of evaporation of reaction fluids, protection of the biological sample from extraneous environmental contamination, and the ability to perform in situ PCR. Various aspects of the design aid in removing trapped air from the reaction fluids and in adding fluids to the biological sample. One embodiment comprises a coverstip with a soft top which aids in prevention of tissue degradation by preventing pressure buildup during PCR.

Abstract: Automated staining equipment that can mix reagents is used to spray a Romanowsky stain onto slide mounted specimens which are then briefly centrifuged. The centrifugation step removes excess stain leaving only a thin film. Depending on the time of the centrifugation step, most of the organic solvent and part of the water in the stain are evaporated by airflow through the equipment. This greatly accelerates the staining reaction and preserves water soluble structures such as the granules in basophilic leukocytes. For optimal performance, this staining procedure requires a thiazin-eosin stain with about 90% to about 40% organic solvent, such as methanol, and only about 10% to about 60% water. This is a unique staining reagent in Romanowsky staining.

Abstract: A low temperature melt film such as EVA is prepared for laser capture microdissection by having a thin specimen non-adhering coating in the range of 0.1% to 10% of the total film thickness placed on the sample exposed side of the film. When the film is brought into contact with the specimen, the specimen non-adhering coating prevents non-specific transfer due to sticky adherence of portions of the sample. At the same time, the non-adhering coating on the low temperature melt film surface can stabilize and protect the low temperature melt film against variations in performance due to ambient humidity and temperature variation. Upon appropriate heating for laser capture microdissection, the barrier of the thin coating allows conventional film melting with otherwise uninhibited adhesion of selected cell areas to the film.

Abstract: In a preferred embodiment, a microplate cassette, including: a generally hollow housing to contain therein a plurality of microplates; and a memory device associated with the cassette and adapted to be placed in operational contact with a portion of a processing device.

Abstract: A method for fabricating a chemical array with multiple features. The method may include ejecting drops from an ejection head spaced from a substrate surface and during movement relative to the substrate surface, onto the substrate surface while varying an ejection velocity of the drops according to a predetermined pattern. An apparatus and computer program product which can execute such the foregoing method are also provided.

Abstract: The present invention is a method and an apparatus to provide a dynamic matrix system for synthesizing a plurality of chemical compounds simultaneously, i.e. in parallel, and to synthesize a series of plurality of simultaneously synthesized chemical compounds sequentially, i.e. in series. The apparatus includes a base support structure, a physical chemistry teabag support structure, a plurality of physical chemistry teabags and a fixed-reactant/liquid reactant mixture shifting (changing) mechanism. The base support structure has a plurality of reaction vessels arranged in at least a two dimensional predetermined array. The physical chemistry teabag support structure is adapted to hold and support a plurality of physical chemistry teabags arranged in at least a two dimensional predetermined teabag array, at least partially coinciding with the base support structure reaction vessel array. The teabags have at least one predetermined fixed reactant thereon.

Abstract: A sample chamber is formed by a housing sealed against a microscope slide. The housing has fluid ports, including a well formed over at least one port. In a rinse station, rinse solution is drawn from a reservoir through the chamber to a waste reservoir. At a fill station, an aliquot of reagent already placed in the well is driven into the chamber. The reagent may be driven into the chamber by first drawing a vacuum on the chamber through the aliquot of reagent and then releasing the reagent to be drawn into the chamber by the vacuum.

Abstract: The present invention provides a method and an apparatus for facilitating the creation and study of biological substrates. In particular, the present invention allows the location of materials deposited on a substrate to be identified, and communicated with great precision. This in turn allows additional biological materials to be deposited as probes over target locations. The present invention also allows for small regions of biological materials deposited on a substrate to be identified and repeatedly accessed, even when the biological substrate has been removed from the device originally used to review the region of interest and is then reinserted into the original device. Furthermore, the present invention allows a region of interest to be accurately located even using a machine that is different from the machine originally used to identify the region of interest.

Abstract: The present invention relates to cost effective analytical instruments for determining the presence or amount of an analyte in a sample. The analytical instruments utilize an assay cartridge which has a sample receiving port and a rotatable carousel containing a plurality of reagent wells. Each reagent well includes a piston element for delivery of reagent to a test surface. The instrument is capable of indexing the assay cartridge to deliver sample and reagents to a test surface in a predetermined and flexibile manner, thus providing an assay protocol which is specific to the type of sample under analysis. The invention also relates to components, features, disposables, reagent delivery systems, accessories, and methods for using such instruments. Appropriate applications include infectious disease testing, cancer detection and monitoring, therapeutic drug level monitoring, allergy testing, environmental testing, food testing, diagnostic testing of human and veterinary samples, and off-line process testing.

Abstract: Multilayer reagent test strips that include at least one hydrophobic fluid flow delay layer, as well as methods for using the same, are provided. The hydrophobic fluid flow delay layer of the subject test strips is one that has been treated with an non-polar organic solvent to provide for a layer which delays fluid flow through a multilayer reagent test strip in a reproducible manner. Also provided are kits and systems that include the subject test strips and find use in practicing the subject methods. The subject compositions and methods find use in a variety of different analyte detection applications.

Abstract: Devices for determining the concentration of an analyte in a physiological sample are provided. The subject devices include a calibration means, at least one light source, a photometric detector array having at least one calibration detector and at least one other detector. The at least one calibration detector is capable of detecting a calibration mark from an analyte concentration measurement device container for calibrating the analyte concentration determination device. The at least one other detector is used for detecting reflected light from an analyte concentration measurement device associated with the analyte concentration determination device. The means for calibrating a component, aspect or feature of the analyte concentration determination device is based on the calibration mark. The subject invention also includes methods for calibrating a component, aspect or feature of a subject device based on the detected calibration mark. Also provided are kits for use in practicing the subject methods.

Abstract: The present invention relates to a gravitational flow purification system. More particularly, the invention relates to a process for purifying or isolating one or more substances from samples comprising said substances. Even more particularly, the invention relates to purifying or isolating macromolecules from biological samples using a gravitational flow apparatus.

Abstract: A holder for an array unit having a planar substrate and an array of chemical moieties on a surface of the substrate. The holder may include a body with a retaining mechanism which releasably retains an array unit in a seated position. A holder identifier may include data on a characteristic of the holder or seated array or be linkable to a file containing such information. An apparatus, method, and computer program product which may be used with such a holder are also provided.

Abstract: Apparatus and methods for automatically staining or treating multiple tissue samples mounted on slides are provided, in which the slides and reagent bottles are held in fixed position, and the reagent, wash and coverslipping solutions brought to the slides. Alternatively, the slides are held in fixed position, while the reagent, wash and coverslipping solutions brought to the slides.

Abstract: An automatic stainer for staining objects, arranged on slides for microscopic examination is described. The automatic stainer has multiple reagent containers arranged one behind another for treating the objects. The slides pass through the reagent containers in succession, a transport basket for receiving multiple slides being provided. Multiple transport baskets can be received simultaneously in respective different reagent containers, and are simultaneously lifted out of the respective reagent container by way of a motorized transport mechanism having a lifting device and are respectively transported on into an adjacent reagent container. A removal station that has a collecting reagent container for the simultaneous reception of multiple transport baskets is arranged at the end of the row of reagent containers.

Abstract: Devices for containing at least one test strip and dispensing a single test strip at a time and methods of using the same are provided. The subject devices are characterized by having a housing that includes a slit configured to be permissive of a single test strip at a time and at least one planar surface to align a test strip with the slit when the device is appropriately agitated. In the subject methods, a subject device with at least one test strip therein is provided and agitated in a manner that causes the at least one test strip to be positioned in an appropriate orientation relative to the slit, wherein a single test strip is caused to exit the housing through the slit as a result of the agitation. Also provided are kits that include at least one subject device.

Abstract: A device for depositing cells on an analytical plate includes a reception chamber which is to be placed above the analytical plate and whose bottom is open, and a material for absorbing a fixative in a cell suspension in the reception chamber. The absorbent material has a hole therein whose interior wall forms an extension of the reception chamber that defines a gap between the reception chamber and the analytical plate through which the cell fixative is absorbed.

Abstract: The drop-by-drop evaporation of a liquid or solution is controlled by monitoring the disappearance of each successive droplet and by actuating the deposition of the next droplet until the desired volume is deposited. In the case of a solution, non-volatile residue (NVR) is collected on a deposition surface plate as a relatively small mound. One of a variety of methods may be employed to measure the evaporative behavior of each droplet and to key the deposition procedure. The process is preferably carried out employing a clean deposition surface plate that is maintained at or below the boiling point of the particular liquid or solvent being deposited. The environment is preferably controlled so that inadvertent contamination is precluded from interfering, and thus the method permits the automatic, micro-processor controlled evaporation of liquids with the resultant deposition of non-volatile residues from solutions within relatively short periods of time.

Abstract: A system for holding a slide. The system includes a housing having a side wall and a top. The top includes a recess surrounded by an outer rim. The system also includes an inlet port in communication with the recess and an elevating mechanism capable of receiving the slide and for raising the slide toward the top of the housing to engage the slide with the outer rim to form an analytical cavity. Together these elements form an analytical cavity in which the assay may be performed.

Abstract: An automated slide stainer with fluid flow control. The fluid flow control controls the flow rate of fluid, e.g., water, applied to at least one slide by the slide stainer. In an automated slide stainer that applies reagents to slides to stain biological specimens on the slides, the flow rate controlled fluid can be used to adequately rinse the slides without damaging the biological specimens contained on the slides.

Abstract: Apparatus and methods for automatically staining or treating multiple tissue samples mounted on microscope slides are provided. Individualized slide temperature control is accomplished by the heating system according to the present invention that has thermal platforms radially mounted to the carousel for heating the slides and sensing the temperature of each. The heating system also permits automated de-waxing if necessary.

Abstract: An automated system for preparing a plurality of cytological specimens from a plurality of fluid samples in vials includes an apparatus for collecting a monolayer of cells from each sample and transferring the cells to a microscope slide for fixing, staining, and inspection. The system includes a first loading station for receiving the sample vials, a second loading station for receiving consumables such as filter membranes, a slide dispenser, and an unloading area for removing completed specimen slides. To maintain one-to-one correlation between the samples and specimens produced therefrom, the system includes a subsystem for identifying each sample and permanently marking each slide with corresponding indicia prior to transferring the specimen thereto.

Abstract: An automated staining system and a reagent container designed for use with the automated staining apparatus. The reagent container includes a reagent containment section capable of containing a volume of a reagent. The reagent containment section includes an upper wall and a base wall that are spaced apart along an axis. The base wall includes a well having a nadir that is aligned axially with an access opening in the upper wall so that a reagent probe entering the opening parallel to said axis will travel toward the nadir. In another aspect of the invention, the reagent container may include a two-dimensional data element containing reagent information. The staining apparatus may include one removable drawer for holding reagent containers and another removable drawer holding slides.

Abstract: An automated system and method for individually processing multiple specimens of particulate matter-containing liquid in respective containers. The containers are transported seriatim along a processing path to present them to, at least, a preprocessing apparatus (e.g., a mixing head), and then to a specimen acquisition apparatus, which removes preprocessed specimen fluid from the container for subsequent analytical testing or evaluation. Each apparatus is actuated in response to presentation of a container thereto so as to carry out its respective operation independently. An exemplary system can include, in sequential order, stations for container loading and unloading, container uncapping and cap disposal, specimen mixing, filter loading, specimen acquisition (e.g., by aspiration, and then slide printing), filter disposal, and container resealing.

Abstract: An automated system for preparing a plurality of cytological specimens from a plurality of fluid samples in vials includes an apparatus for collecting a monolayer of cells from each sample and transferring the cells to a microscope slide for fixing, staining, and inspection. The system includes a first loading station for receiving the sample vials, a second loading station for receiving consumables such as filter membranes, a slide dispenser, and an unloading area for removing completed specimen slides. To maintain one-to-one correlation between the samples and specimens produced therefrom, the system includes a subsystem for identifying each sample and permanently marking each slide with corresponding indicia prior to transferring the specimen thereto.

Abstract: Apparatus and method for processing specimens, e.g., biological specimens, to extract samples for both liquid (i.e., extracellular) and slide-based (i.e., intracellular) testing. Both types of samples can be obtained from a single fluid specimen. A fluid sampling station removes fluid from a specimen container and places it in a sample receptacle. A specimen acquisition station removes fluid from the container, separates particulate matter (e.g., cells) from the removed fluid, and forms a sample layer of particulate matter, which is transferred to a slide. The two sampling operations can be carried out in any order. The fluid sample receptacle may have a special one-way valve arrangement. The apparatus can be automated so as to process multiple fluid specimens in their respective containers. The machine according to this invention is a “platform instrument” that can produce all required liquid samples and slide-based samples for essentially all cytopathology tests.

Abstract: The present invention relates to an apparatus for detecting nucleic acid molecules such as target DNA molecules and mRNA molecules by using a DNA probe, and provides a DNA capillary, comprising a fluid passageway formed of a cylindrical capillary made of glass, a plurality of independent probe regions formed in the inner wall of the fluid passageway, and DNA probes each immobilized in the probe region, the immobilized DNA probes differing from each other. For performing the measurement, a sample is introduced through an open portion into the capillary so as to perform reaction and, then, fluorimetry.

Abstract: An automated slide stainer with slides mounted in a horizontal position on a rotary carousel. Reagents and rinse liquids are automatically dispensed onto tissue sections or cells mounted on slides for the purpose of performing chemical or immunohistochemical stains. The rinse liquids are removed by an aspiration head connected to a source of vacuum. Individual slides or groups of slides are supported on flat heating stations for heating to individual temperatures. Temperature control electronics on the carousel are controlled by a user interface off of the carousel.

Abstract: A clinical analyzer where incoming samples are partitioned into groups in accord with the length of time required for the assay to be completed or in accord with the pattern of reagent addition(s) taken with length of time required for the assay to be completed. Medium length time assays are completed, removed from a reaction carousel and replaced by shorter length time assays during a single operational cycle in which longer length assays are also completed.

Abstract: An automated in situ heat induced antigen recovery and staining method and apparatus for treating a plurality of microscope slides. The process of heat induced antigen recovery and the process of staining the biological sample on the microscope slide are conducted in the same apparatus, wherein the microscope slides do not need to by physically removed from one apparatus to another. Each treatment step occurs within the same reaction compartment. The reaction conditions of each reaction compartment for treating a slide can preferably be controlled independently, including the individualized application of reagents to each slide and the individualized treatment of each slide. The reagents are preferably held in a reagent dispensing strip similar to a “blister pack”.

Abstract: In a test strip measuring method in which a coloration measurement is conducted while a test strip (4) is being moved, there are detected the optical characteristics R of the ground of a test strip and the optical characteristics T of a test line (4b) which has appeared on the test strip, and the test strip is judged based on the difference or ratio between R and T. Even though the ground of the test strip presents variations in optical characteristics, and even though there are variations among samples or among test strips, such variations can be absorbed, thus assuring an accurate judgment.

Abstract: A clinical analyzer where incoming samples are partitioned into groups in accord with the length of time required for the assay to be completed or in accord with the pattern of reagent addition(s) taken with length of time required for the assay to be completed. Medium length time assays are completed, removed from a reaction carousel and replaced by shorter length time assays during a single operational cycle in which longer length assays are also completed.

Abstract: A method and a device for removing an analytic consumable product, in particular a test element, from a storage container having chambers which are sealed by foils from which the consumable product is pushed out by means of a plunger (7) can be optimized in that the magnitude of the thrusting force exercised by the plunger (7) during its forward motion can be controlled in dependence on the plunger (7) position.

Abstract: A testing device for analyzing the glucose concentration of a sample of blood is adapted to remove a test sensor from a sensor package. The testing device comprises an inlet region and a puncturing member The inlet region receives a portion of the sensor package extending inward from an outer periphery of the test sensor package. The puncturing member is adapted to extend into the inlet region, puncture the sensor package, and to engage a mating feature of the test sensor. The puncturing member is adapted to hold the test sensor in the inlet region in a manner allowing the package to be removed and is adapted to hold the test sensor in the inlet region during testing a blood sample.

Abstract: An automatic analyzer system including transport means for moving sample racks within the system. In order to simplify and reduce the cost of the means for transporting the sample racks the system comprises (a) a rack supply unit capable of containing sample racks, said rack supply unit including (a.1) a rack input device for introducing sample racks into the rack supply unit, (a.2) a rack output device for removing sample racks from the rack supply unit, (a.3) a buffer unit for storing unprocessed racks before they are transferred from said rack supply unit to a position corresponding to an analyzer unit, and for storing also already processed racks which contain samples having a probability of being reexamined, and (a.

Abstract: A sensor dispensing instrument adapted to handle a sensor pack containing a plurality of sensors and to perform a test using one of the sensors, wherein the sensor dispensing instrument includes an electronics assembly for performing the test and displaying test results. The electronics assembly includes a printed circuit board having electrical components, at least one button, and a liquid crystal display mounted thereon. The electronics assembly is formed and tested prior to assembling the electronics assembly into the outer housing of the sensor dispensing instrument.

Abstract: A sensor dispensing instrument adapted to handle a sensor pack containing a plurality of sensors and to perform a test using one of the sensors. The sensor dispensing instrument includes an outer housing and a mechanical mechanism contained therein for rotating the sensor pack and ejecting one of the sensors from the sensor pack and through a sensor slot on the housing. The mechanical mechanism of the sensor dispensing instrument is operated by first moving a disk drive pusher in a first direction to rotate the sensor pack, and then moving the disk drive pusher in a second direction to eject a sensor from the sensor cavity and through the sensor slot.

Abstract: A method and a device for removing an analytic consumable product, in particular a test element, from a storage container having chambers which are sealed by foils from which the consumable product is pushed out by means of a plunger (7) can be optimized in that the magnitude of the thrusting force exercised by the plunger (7) during its forward motion can be controlled in dependence on the plunger (7) position.

Abstract: An automated workstation capable of continuous, non-stop processing of specimens includes an environmentally controlled storage area that holds multiple cassettes containing specimen plates. A robotic arm for processing the specimens, e.g., by grasping the plates, moving them from the cassettes to other apparatus contained within the workstation, and placing the plates back in the cassettes. An interlock mechanism prevents the operator and robotic arm from simultaneously accessing a cassette. Novel robotic arms, robotic arm positioning mechanisms, plate handling mechanisms, effector tip/plate washing mechanisms, thin-walled pipetters, back-flushing mechanisms and fluid level detection mechanisms, as well as methods for operating the same, facilitate continuous operation of the workstation along with compactness, high throughput and high accuracy of operation. Narrow, thin-walled capillary-like pipetters serve as both means for acquiring and processing small quantity specimens with high precision.

Abstract: A DNA probe synthesis system may include a target holder for holding a target chip, an ejector array chip, a wash and dry station, and conveyance means for moving the target holder and the chip between the ejector array chip and the wash and dry station. The ejector array chip may include ejectors, reservoirs for containing DNA bases, and microchannels all on the same substrate. The ejectors may be Self Focusing Acoustic Transducers (SFATs).

Abstract: Apparatus and methods for controlling the fluid on a slide are provided. Fluid reduction is accomplished by directing stream(s) of fluid at an edge of the slide, the streams of fluid being at an angle with the slide of less than 90°. The surface tension at the edge of the slide is broken by the stream(s). And, the fluid which is on the slide is drawn or pulled by the streams of liquid, thereby reducing the fluid on the slide to a reproducible, consistent level.

Abstract: An apparatus is provided to automatically cover and uncover crucibles according to a predetermined procedure in a proximate analyzer. A series of crucibles mounted in a first carousel is heated in a furnace. A second carousel mounted above the first carousel holds crucible covers. A mechanism synchronizes the movements of the carousels so that the heated crucibles are automatically covered and uncovered at the appropriate times during the analysis with a corresponding cover by lowering or raising the second carousel. The movements of both carousels are automatically controlled so that at appropriate points in the testing cycle they rotate simultaneously about a common central axis and a crucible is deposited on a weighing platform by controlling the vertical motion of the entire carousel apparatus. The crucible is weighed either with or without a crucible cover depending on the stage of the analysis without the need of manual intervention.

Abstract: Disclosed is an automated staining apparatus including an arm (30) moveable in three dimensions, and a hollow tip head (70) located on the arm including integral reagent tip head (40), wash tip (41) and blow tip (42) for selectively dispensing gas and liquid onto microscope slides. Also disclosed are various sub-components of the apparatus that are specifically adapted to the processing of specimens on slides.

Abstract: A system and method for applying one or more chemicals to a tissue sample is provided. The system preferably includes a cassette for housing a slide device, a film, and an injection system. The slide device preferably includes a specimen slide for containing the tissue sample and a cover plate connected to the specimen slide. The film is preferably moveable through the cassette along guide rollers and preferably contains a plurality of containers containing one or more chemicals. The injection system may include a piston for displacing the chemicals from the containers through an injection port to the tissue sample. The cassette may be placed on a cassette driver that contains a motor-driven shaft for driving the piston and moving the film.

Abstract: A method and a device for removing an analytic consumable product, in particular a test element, from a storage container having chambers which are sealed by foils from which the consumable product is pushed out by means of a plunger (7) can be optimized in that the magnitude of the thrusting force exercised by the plunger (7) during its forward motion can be controlled in dependence on the plunger (7) position.

Abstract: Apparatus and methods for controlling the fluid on a slide are provided. Fluid reduction is accomplished by directing stream(s) of fluid at an edge of the slide, the streams of fluid being at an angle with the slide of less than 90°. The surface tension at the edge of the slide is broken by the stream(s). And, the fluid which is on the slide is drawn or pulled by the streams of liquid, thereby reducing the fluid on the slide to a reproducible, consistent level.

Abstract: Whether or not there remains a frameless chemical analysis film in a cartridge in which a plurality of the frameless chemical analysis films are stacked is judged by a film presence detector disposed in a second position different from a position where a film takeout mechanism takes out the frameless chemical analysis films from the cartridge so that the film presence detector does not interfere with the film takeout mechanism.

Abstract: Centrifugal analyzer and method for staining biological or non-biological samples in microgravity, wherein the method utilizes an increase in weight of a fluid sample as a function of g-load, to overcome cohesive and frictional forces from preventing its movement in a preselected direction. Apparatus is characterized by plural specimen reservoirs and channels in a slide, each channel being of differing cross-section, wherein respective samples are selectively dispensed, from the reservoirs in response to an imposed g-factor, precedent to sample staining. Within the method, one thus employs microscope slides which define channels, each being of a differing cross-section dimension relative to others. In combination therewith, centrifugal slide mounting apparatus controllably imposes g-vectors of differing magnitudes within a defined structure of the centrifuge such as a chip array.

Abstract: A method and apparatus for dispensing precise quantities of reagents is disclosed including a positive displacement syringe pump in series with a dispenser, such as an aerosol dispenser or solenoid valve dispenser. The pump is controlled by a stepper motor or the like to provide an incremental quantity or continuous flow of reagent to the dispenser. The pump and dispenser are operated in cooperation with one another such that the quantity and/or flow rate of liquid dispensed by the dispenser can be precisely metered substantially independently of the particular operating parameters of said dispenser to attain a desired flow rate, droplet size or mist quality, droplet frequency and/or droplet velocity.